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Flexible Design and Low Power for Ultrasound Systems

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Dallas, TX, 75243
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This entry was posted on Friday, January 8th, 2010 at 3:39 pm and is filed under Videos / Podcasts.

A New Approach to Verifying and Validating Medical Device Development
The list of features in medical devices is rapidly rising: Even the simplest of medical devices—such as diagnostic and monitoring systems—house more and more system components, which add greater functionality to the device at a low cost. But by adding components, device software becomes complex and burdens compliance testing and premarket certification activities, such as 510(k) submissions mandated by the U.S. Food and Drug Administration (FDA).
Demystifying DO-254
Interest in DO-254 first occurred in Europe and has since spread to the US commercial aircraft industry. If you are being asked about your company’s DO-254 direction and compliance, but have been overwhelmed with information on the subject, then this article is for you.
TI’s Medical Applications Guide
Download TI’s Medical Applications Guide to view system block diagrams for a broad range of medical applications and find device details and design resources.